Clinical relevance of the TECTA c.6183G>T variant identified in a family with autosomal dominant hearing loss: a case report

por Sansović, Ivona, Meašić, Ana-Maria, Odak, Ljubica, Kero, Mijana
Publicado 2023

Neurodevelopmental disorder caused by an inherited novel KMT5B variant: case report

por Odak, Ljubica, Vulin, Katarina, Meašić, Ana-Maria, Šamadan, Lara, Batoš, Ana Tripalo
Publicado 2023

Trends in the treatment of undescended testes: a pediatric tertiary care center experience from Croatia

por Bašković, Marko, Zaninović, Luca, Sansović, Ivona, Meašić, Ana Maria, Katušić Bojanac, Ana, Ježek, Davor
Publicado 2022